Novel synthesis and crystallization of piperazine ring-containing compounds

ABSTRACT

The present invention is directed to methods for the preparation of piperazine ring-containing compounds, particularly mirtazapine. According to the present invention, the mirtazapine intermediate 1-(3-carboxypyridyl-2)-4-methyl-2-phenyl-piperazine is made by hydrolyzing 1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine with a base where the base is present in a ratio of up to about 12 moles of the base per one mole of 1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine. The mirtazapine intermediate 1-(3-carboxypyridyl-2)-4-methyl-2-phenyl-piperazine may be made by hydrolyzing 1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine with potassium hydroxide at a temperature of at least about 130° C. The method of the present invention also includes reacting 2-amino-3-hydroxymethyl pyridine with N-methyl-1-phenyl-2,2′-iminodiethyl chloride to form 1-(3-hydroxymethylpyridyl-2)-4-methyl-2-phenyl piperazine, and adding sulfuric acid to the 1-(3-hydroxymethylpyridyl-2)-phenyl-4-methylpiperazine to form mirtazapine. The present invention also relates to new processes for recrystallization of mirtazapine from crude mirtazapine.

CROSS-REFERENCE TO RELATED APPLICATION

[0001] This application claims the benefit of U.S. ProvisionalApplication No. 60/130,047, filed Apr. 19, 1999.

FIELD OF THE INVENTION

[0002] The present invention relates to synthetic organic chemistry,particularly, to synthesis of piperazine ring-containing compounds, suchas mirtazapine, and to the crystallization of mirtazapine from differentsolvents and solvent systems.

BACKGROUND OF THE INVENTION

[0003] Mirtazapine, 1,2,3,4,10,14b-hexahydro-2-methyl-pyrazino[2,1-a]pyrido[2,3-c][2] benzazepine, having the formula I:

[0004] is approved, under the trademark Remeron®, by the U.S. Food andDrug Administration, for the treatment of depression. Mirtazapine has atetracyclic chemical structure unrelated to other classes ofantidepressants such as selective serotonin reuptake inhibitors,tricyclics or monoamine oxidase inhibitors. Mirtazapine belongs to thepiperazinoazepine group of compounds.

[0005] Mirtazapine may be made by methods described in U.S. Pat. No.4,062,848. By a process of U.S. Pat. No. 4,062,848 (“the '848 patent”),the mirtazapine intermediate1-(3-hydroxymethylpyridyl-2-4-methyl-2-phenyl-piperazine is made by athree step process starting with a 2,3-substituted pyridine derivative.Therefore, as shown in Scheme 1, when starting with2-amino-3-cyano-pyridine, the process of the '848 patent requires foursynthetic steps to make mirtazapine. It is desirable to have a processfor making mirtazapine that requires fewer steps, and therefore requiresless reagent, solvent and time.

[0006] By the process of U.S. Pat. No. 4,062,848 (“the 848 patent”), themirtazapine intermediate1-(3-carboxypyridyl-2)-4-methyl-2-phenyl-piperazine is made by thehydrolysis of the nitrile1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine under highly basicconditions of 25 moles of potassium hydroxide (KOH) per mole of nitrile,at high temperature and for long reaction times of 24 hours. These harshreaction conditions necessitate a great effort in purifying theresulting product as well as creating environmental waste disposalissues associated with neutralizing and disposing of large volumes ofconcentrated basic solutions. The highly basic conditions and longreaction times make the procedure of the '848 patent very costly,especially in terms of reactor time.

[0007] According to the methods of U.S. Pat. No. 4,062,848, crudemirtazapine is recrystallized only in ether and petrol ether 40-60. Thesolvents ether and petrol ether 40-60 are both very difficult to handlein large scale production.

SUMMARY OF THE INVENTION

[0008] The present invention is directed to a method for the preparationof mirtazapine, comprising the steps of: reacting a compound of theformula

[0009] with a compound of the formula

[0010] to form a compound of the formula

[0011] adding a ring closing reagent to the compound of the formula

[0012] to form mirtazapine, wherein R¹ is selected from the groupconsisting of hydroxymethyl, chloromethyl, bromomethyl and iodomethyl;R² is amine; and R³ is selected from the group consisting of chloro,fluoro, bromo and iodo.

[0013] In a preferred embodiment of the present invention is directed toa method for the preparation of mirtazapine, comprising the steps ofreacting 2-amino-3-hydroxymethyl pyridine withN-methyl-1-phenyl-2,2′-iminodiethyl chloride to form1-(3-hydroxymethylpyridyl-2)-4-methyl-2-phenyl piperazine, and addingsulfuric acid to the1-(3-hydroxymethylpyridyl-2)-4-methyl-2-phenyl-piperazine to formmirtazapine.

[0014] Further, it has now been discovered that the mirtazapineintermediate 1-(3-carboxypyridyl-2)-4-methyl-2-phenyl-piperazine may bemade by hydrolysis of the nitrile1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine using new morefavorable reaction conditions. The new reaction conditions of thepresent invention include a low mole to mole ratio of potassiumhydroxide to nitrile and shorter reaction times.

[0015] The present invention relates to a improved process for making1-(3-carboxypyridyl-2)-4-methyl-2-phenyl-piperazine by hydrolyzing1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine comprising the step ofreacting 1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine with a basewherein the base is present in a ratio of up to about 12 moles of thebase per one mole of 1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine.

[0016] In a preferred embodiment of the present invention, the ratio ofthe base to 1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine is about12 moles of base to about one mole of1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine to about 9 moles ofbase to about one mole of1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine.

[0017] In another preferred embodiment of the present invention, thebase is potassium hydroxide or sodium hydroxide.

[0018] In another embodiment of the present invention, the mixture ofthe 1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine and the base isheated to at least about 130° C.

[0019] In another embodiment of the present invention, the hydrolysis of1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine is carried out in amixture water and a solvent selected from the group consisting ofmethanol, ethanol, propanol, isopropanol, butanol, dimethylformamide,dimethylacetamide and dimethylsulfoxide.

[0020] The present invention also relates to improved processes formaking mirtazapine from crude mirtazapine comprising the steps of (a)heating a mixture of crude mirtazapine and solvent; and (b) isolatingmirtazapine.

[0021] In a preferred embodiment of the present invention, water isadded to the heated mixture of mirtazapine and solvent to facilitateprecipitation of mirtazapine.

[0022] In an additional embodiment of the present invention, preferredsolvents are methanol, ethanol, isopropanol, acetone, toluene, andhexane and mixtures thereof.

[0023] In an additional embodiment of the present invention, preferredsolvents are toluene, hexane, and methylene chloride.

DETAILED DESCRIPTION OF THE INVENTION

[0024] The present invention relates to a novel process for preparingpiperazine ring-containing compounds, such as mirtazapine, as describedin Scheme 2 below. The process of the present invention is advantageousover prior art processes due to, inter alia, the higher yield, smallernumber of steps in relation to the alternative methods, and minimizedraw material costs.

[0025] More particularly, the present invention relates to the processof making mirtazapine from compounds of the formulae II, III and IV. Inthe process of the present invention the compound of formula II inScheme 2 above, wherein R¹ denotes hydroxymethyl, chloromethyl,bromomethyl or iodomethyl, and R² denotes amine, preferably —NH₂, isreacted with the compound of formula III in Scheme 2 above, wherein R³denotes chloro, fluoro, bromo or iodo, to form the compound of formulaIV wherein R¹ is defined as above.

[0026] In the process of the present invention, the compound of formulaII is dissolved in a solvent such as methylene chloride. The compound offormula III is added to the solvent mixture and the resulting mixture isheated. Preferably the reaction mixture is heated to the refluxtemperature of the solvent. The mixture is heated to form the compoundof formula IV. Mirtazapine is then prepared by ring closure of thecompound of formula IV. Ring closure of the compound of formula IV maybe performed using a ring-closing reagent. Suitable ring closingreagents are dehydrating or dehydrohalogenating agents. Dehydrating ordehydrohalogenating agents that may be added to the reaction mixture forthis purpose include acids, such as sulfuric acid, concentrated sulfuricacid, concentrated hydrochloric acid, trifluoroacetic acid, phosphoricacid, polyphosphoric acid (PPA), phosphorus oxychloride, phosphorustrioxide, phosphorus pentoxide and Lewis acids, such as aluminumchloride, ferric chloride, zinc chloride, tin chloride, titaniumchloride, boron trifluoride, antimony pentachloride and zirconiumtetrachloride.

[0027] Dehydrating agents that are particularly preferred are sulfuricacid and phosphorus derivatives, such as PPA and phosphorus oxychloride.Concentrated sulfuric acid most preferred. A particularly preferreddehydrohalogenating agent is aluminum chloride.

[0028] In a preferred embodiment of the present invention the compoundsof the formulae II, III and IV are compounds of the formulae II′, III′and IV′ respectively as shown in Scheme 3 below. In an embodiment of thepresent invention, 2-amino-3-hydroxymethyl pyridine is reacted withN-methyl-1-phenyl-2,2′-iminodiethyl chloride to form1-(3-hydroxymethylpyridyl-2)-4-methyl-2-phenyl-piperazine. In thepresent invention, 2-amino-3-hydroxymethyl pyridine (II′) is added to asolvent. Suitable solvents include 1,2-dichloroethane, methylenechloride, dimethylformamide, dimethylacetamide and dimethylsulfoxide.N-Methyl-1-phenyl-2,2′-imidodiethyl-chloride (III′) is added to thesolvent mixture and the resulting mixture is heated. Preferably thereaction mixture is heated to the reflux temperature of the solvent. Themixture is heated until1-(3-hydroxymethylpyridyl-2)-4-methyl-2-phenyl-piperazine is formed andthe reaction is complete. A suitable time is about six to about 24hours. The 1-(3-hydroxymethylpyridyl-2)-4-methyl-2-phenyl-piperazine isthen converted to mirtazapine by ring closure.

[0029] The ring closure of1-(3-hydroxymethylpyridyl-2)-4-methyl-2-phenyl-piperazine is performedunder strongly dehydrating (R¹=OH) conditions, preferably at an elevatedtemperature. Suitable dehydrating agents, include acids, such assulfuric acid, concentrated hydrochloric acid, trifluoroacetic acid,phosphoric acid, polyphosphoric acid (PPA), phosphorus oxychloride,phosphorus trioxide and phosphorus pentoxide. Dehydrating agents thatare particularly preferred are sulfuric acid and phosphorus derivatives,such as PPA and phosphorus oxychloride. Concentrated sulfuric acid ismost preferred.

[0030] The present invention also provides new processes for making themirtazapine intermediate1-(3-carboxypyridyl-2)-4-methyl-2-phenyl-piperazine from the nitrile1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine where the nitrile is(I) hydrolyzed by base using a new low mole to mole ratio of base to thenitrile 1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine and (ii)hydrolyzed using short reaction times.

[0031] Where the present invention provides improved methods for makingthe mirtazapine intermediate1-(3-carboxypyridyl-2)-4-methyl-2-phenyl-piperazine, the nitrile1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine is dissolved in amixture of water and organic solvent. Preferred organic solvents includepolar aprotic solvents and alcohols. Polar aprotic organic solvents suchas dimethylformamide, dimethylacetamide and dimethylsulfoxide and thelike are preferred. Preferred alcohols are methanol, ethanol, propanol,isopropanol, butanol and the like. A suitable amount of base, such aspotassium hydroxide or sodium hydroxide, is added to the reactionmixture. An amount of base, such as potassium hydroxide or sodiumhydroxide, of up to about 12 moles of base per mole of nitrile (forexample 12:1 KOH:nitrile) is preferred. Amounts of base, such aspotassium hydroxide, in the ratio of about 9 moles of potassiumhydroxide per one mole of nitrile (9:1 KOH:nitrile), to about 12 molesof potassium hydroxide per mole of nitrile (12:1 KOH:nitrile) arepreferred.

[0032] In the present invention, the mixture of the nitrile1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine, solvent and base isheated to at least about 130° C. Reaction temperatures of about 130° C.to about 150° are preferred. In an embodiment of the present invention,the reaction may be conducted under pressure to facilitate theattainment of high temperatures. A pressure of at least about 3atmospheres is preferred. Pressures of at least about 3 atmospheres toabout 4 atmospheres are more preferred. The reaction mixture is heateduntil the reaction is complete. The completion of the reaction may bemonitored by HPLC. The amount of time needed for the completion of thehydrolysis of the nitrile varies with the temperature of the reaction.Higher reaction temperatures generally require shorter reaction times,while lower reaction temperatures generally requires longer reactiontimes. While not limiting the reaction time of the present invention,preferred reaction times of the present invention may be from about 2hours to about 8 hours. Upon completion of the reaction, the pH of thereaction mixture is lowered, preferably to a pH of about 6 to about 7.Preferably the pH is lowered with hydrochloric acid. The mirtazapineintermediate, 1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine isisolated following washing and filtration of the reaction mixture.

[0033] In an additional embodiment of the present invention, thereaction mixture of the nitrile1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine, and potassiumhydroxide, is heated while using a minimum amount of water, such asabout 0.25-1 mL of water per gram of KOH, and small amounts of anaprotic solvent such as dimethylformamide, dimethylacetamide anddimethylsulfoxide, such as about 0.1 to 0.5 grams of aprotic solvent pergram of nitrile, under very concentrated conditions or almost neatconditions at atmospheric pressure. The mirtazapine intermediate,1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine is isolated followingwashing and filtration of the reaction mixture.

[0034] The new processes of the present invention for making themirtazapine intermediate1-(3-carboxypyridyl-2)-4-methyl-2-phenyl-piperazine from the nitrile1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine significantly reducethe quantity of potassium hydroxide used, from 25 moles of potassiumhydroxide per mole of the nitrile as in the '848 patent, to about 12moles or less of potassium hydroxide to one mole of the nitrile. Thereduction in the amount of base needed considerably simplifies thework-up of the reaction and minimizes environmental problems.

[0035] The present invention also provides new methods for making puremirtazapine by purifying crude mirtazapine by recrystallization. Uponthe ring closure of1-(3-hydroxymethylpyridyl-2)-4-methyl-2-phenyl-piperazine to formmirtazapine, the crude product, mirtazapine, is purified byrecrystallization.

[0036] It has been discovered that common solvents such as toluene ormethylene chloride and solvent systems such as alcohol-water can be usedin the recrystallization of crude mirtazapine. According to the presentinvention, crude mirtazapine is suspended in a suitable solvent.Preferred solvents include methanol, ethanol, isopropanol, and acetoneand mixtures thereof, or mixtures of one or more of those solvents withwater. Additional preferred solvents also include toluene, hexane, andmethylene chloride. Solvent mixtures of water and ethanol are morepreferred. Solvent mixtures of ratios of about 1:1 to about 1:4ethanol:water are preferred.

[0037] In the present invention, the suspension of crude mirtazapine andsolvent is heated to a suitable temperature. Suitable temperaturesinclude, for example, the reflux temperature of the solvent system beingused in any particular embodiment of the present invention. For example,in an embodiment of the present invention where toluene is the solvent,a temperature of about 110° C. is suitable. Purified mirtazapineprecipitates upon cooling of the reaction mixture. Filtration and dryingof the resulting precipitate yields purified, recrystallizedmirtazapine.

[0038] In a further example, crude mirtazapine is suspended in a solventsuch as ethanol, and the mixture is heated to reflux. Water is thenadded dropwise and the solution is cooled to facilitate precipitation ofmirtazapine. The precipitate is purified by filtration, washing anddrying to yield purified mirtazapine. The crystallized mirtazapine maybe a water adduct thereby containing up to 3% water by weight (3% w/w).

[0039] The solvents and solvent systems of the present invention aresuitable for large scale reactions, and are more suitable for largescale reactions than ether or petrol ether 40-60. Additionally, thecrystallization yield can be substantially improved when using thesolvent system of the present invention.

[0040] Mirtazapine and mirtazapine intermediates,1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine and1-(3-carboxypyridyl-2)-4-methyl-2-phenyl-piperazine each contain anasymmetric carbon atom, as a result of which separate optical isomersmay be prepared in addition to a racemic mixtures. Processes of thepresent invention include these optical isomers just as the racemicmixtures are included in the invention.

[0041] In accordance with the present invention, mirtazapine produced bythe process of the present invention may be prepared as pharmaceuticalcompositions that are particularly useful for the treatment ofdepression. Such compositions comprise a therapeutically effectiveamount of mirtazapine with pharmaceutically acceptable carriers and/orexcipients known to one of skill in the art.

EXAMPLES

[0042] The following examples are given for the purpose of illustratingthe present invention and shall not be construed as being limitations onthe scope or spirit of the invention.

Example 1 Preparation of1-(3-Hydroxymethylpyridyl-2)-4-Methyl-2-Phenyl-Piperazine

[0043] In a 50 mL three-necked flask equipped with a mechanical stirrer,a condenser and a thermometer 1 g (0.008 mole) of2-amino-3-hydroxymethyl pyridine and 20 mL of 1,2-dichloroethane werecharged. The mixing is started and to the suspension 2.8 g (0.012 mole)of N-methyl-1-phenyl-2,2′-iminodiethyl-chloride are added. The reactionmixture is heated to reflux (˜80° C.) and maintained at this temperaturefor six hours.

[0044] After six hours the reaction mixture is cooled and the solvent(1,2-dichloroethane) is removed by dry distillation. A yellowish powderis obtained which contains 1.8 g 1-(3-hydroxymethylpyridyl-2)-4-methyl-2-phenyl-piperazine (yield 80%). This powder can beused without additional purification for the preparation of mirtazapine.

Example 2 Preparation of Mirtazapine

[0045] In a 50 mL three-necked flask equipped with a mechanical stirrer,a condenser and a thermometer 1.8 g of 1-(3-hydroxymethylpyridyl-2)-4-methyl-2-phenyl-piperazine are added to ˜5 mL ofconcentrated sulfuric acid that was previously cooled to 10° C. Theobtained solution is mixed at room temperature for 4 hours, then heatedfor one hour to about 50° to 60° C. After cooling, the reaction mass isadded to 25 g of ice under mixing and neutralized with a concentratedammonia solution or sodium hydroxide. The formed precipitate isseparated by filtration. The mother liquor is evaporated to drynessunder vacuum. Both the formed precipitate and the residue from themother liquor are each suspended in ˜20 mL of isopropanol. The combinedisopropanol extracts are evaporated to dryness. An oil is obtained whichcontains 1.35 g of mirtazapine (yield 80%).

Example 3 Preparation of Mirtazapine

[0046] 1-(3-Hydroxymethylpyridyl-2)-4-methyl-2-phenyl-piperazine (1.8 g)is added to ˜5 mL of concentrated sulfuric acid. The resulting solutionis mixed at 35° C. for 6 hours. After cooling, the reaction mixture isadded to 25 g of ice under mixing and basified with a concentratedammonia solution or sodium hydroxide solution to pH=10. The separatedprecipitate is extracted into methylene chloride and the extract isevaporated to dryness; 1.6 g of Mirtazapine is obtained (yield 95%).

Example 4 Preparation of1-(3-Carboxypyridyl-2-)-4-Methyl-2-Phenyl-Piperazine

[0047] 1-(3-cyanopyridyl-2-)-4-methyl-2-phenyl-piperazine (54 g) isdissolved in 340 mL of ethanol and 34 mL of water. Potassium hydroxideflakes, 85% (113 g), are added and the reaction mixture is heated in anautoclave to 140° C. The pressure increases to 3-4 atmospheres and thereaction mixture is maintained under pressure with mixing for 5 hours.After 5 hours, the reaction mixture is cooled, the ethanol is removedfrom the mixture by vacuum distillation, fresh water and toluene areadded and the 2 phases are separated. The water solution is neutralizedwith hydrochloric acid (HCl) to pH=6.5-7. At pH=6.5-7 the water isevaporated and toluene is added. The inorganic salts are filtered andthe toluene solution is evaporated to dryness yielding 52 g of1-(3-carboxypyridyl-2-)-4-methyl-2-phenyl-piperazine (yield: 90%).

Example 5 Preparation of1-(3-Carboxypyridyl-2-)-4-Methyl-2-Phenyl-Piperazine

[0048] Potassium hydroxide (150 g of KOH flakes, 85%) and 75 mL of waterand 6.5 g of DMSO are added to1-(3-cyanopyridyl-2-)-4-methyl-2-phenyl-piperazine (54 g) and thereaction mixture is heated to 145-150° C. and mixed for 8 hours. After 8hours, the inorganic phase containing water and potassium hydroxide(KOH) is separated and the organic phase, containing mainly a productoil, is cooled. Fresh water and toluene are added and the two phases areseparated. The aqueous solution is neutralized with HCl to pH=6.5-7. AtpH=6.5-7, the water is evaporated and toluene is added. The inorganicsalts are filtered and the toluene solution is evaporated to drynessyielding 52 g of 1-(3-carboxypyridyl-2-)-4-methyl-2-phenyl-piperazine(yield: 90%).

Example 6 Recrystallization of Mirtazapine

[0049] Mirtazapine (20 g), obtained as in Examples 2 and 3, is suspendedin 20 mL of ethanol and heated to reflux. At reflux, 40 mL of water isadded dropwise to the solution over one hour followed by cooling to 10°C. The resulting filter cake is washed with a solution of water:ethanol(2:1) and dried at 60° C. under a vacuum. Crystallized mirtazapine, 18g, is obtained in 90% yield.

[0050] Table 1 sets forth a summary of additional experiments generallyfollowing procedures described above wherein the Yield % is the percentyield of mirtazapine crystals from crude mirtazapine and the Purity % isthe percent purity as compared to a mirtazapine standard. TABLE 1Purification of Crude Mirtazapine by Recrystallization Ratio of solventsYield¹ Solvent system ml:ml/g Conditions % hexane 10 reflux 55 toluene 3reflux 32 toluene 2 refiux 53 acetone/water 6:25 25° C. 65 ethanol/water7:10 reflux 67 methanol/water 2.25:1.5 reflux 67 ethanol/water 1.5:2reflux 72 isopropyl/water 1.65:2 reflux 60 acetone-water 3:2 reflux 53ethanol/water 1:1.3 reflux 70 ethanol/water 1.3:1.75 reflux 90.3ethanol/water 1:4 reflux 100 ethanol/water 1.1:1.2 reflux 87.8ethanol/water 0.8:0.9 reflux 90 ethanol/water 0.8:1 reflux 57ethanol/water 0.6:0.7 reflux 89.1 ethanol/water 0.35:0.7 reflux 91.5ethanol/water 0.6:0.69 reflux 87 ethanol/water 2:2.8 reflux 95.6

[0051] Although certain presently preferred embodiments of the inventionhave been described herein, it will be apparent to those skilled in theart to which the invention pertains that variations and modifications ofthe described embodiments may be made without departing from the spiritand scope of the invention. Accordingly, it is intended that theinvention be limited only to the extent required by the appended claimsand the applicable rule of law.

We claim:
 1. A method for the preparation of mirtazapine, comprising thesteps of: (a) reacting a compound of the formula

 with a compound of the formula

 to form a compound of the formula

(b) adding a ring closing reagent to the compound of the formula

 to form mirtazapine wherein R¹ is selected from the group consisting ofhydroxymethyl, chloromethyl, bromomethyl and iodomethyl; R² is amine;and R³ is selected from the group consisting of chloro, fluoro, bromoand iodo.
 2. The method of claim 1 , wherein R¹ is hydroxymethyl, R² is—NH₂, and R³ is chloro.
 3. The method of claim 1 , wherein said a ringclosing reagent is selected from the group consisting of sulfuric acid,concentrated sulfuric acid, concentrated hydrochloric acid,trifluoroacetic acid, phosphoric acid, polyphosphoric acid, phosphorusoxychloride, phosphorus trioxide, phosphorus pentoxide, Lewis acids,aluminum chloride, ferric chloride, zinc chloride, tin chloride,titanium chloride, boron trifluoride, antimony pentachloride andzirconium tetrachloride.
 4. The method of claim 2 , wherein said ringclosing reagent is sulfuric acid.
 5. The method of claim 1 which furthercomprises the step of heating.
 6. A method for the preparation ofmirtazapine, comprising the steps of: (a) reacting2-amino-3-hydroxymethyl pyridine withN-methyl-1-phenyl-2,2′-iminodiethyl chloride to form1-(3-hydroxymethylpyridyl-2)-4-methyl-2-phenyl-piperazine, and (b)adding a ring closing reagent to the1-(3-hydroxymethylpyridyl-2)-4-methyl-2-phenyl-piperazine to formmirtazapine.
 7. The method of claim 6 , wherein said a ring closingreagent is selected from the group consisting of sulfuric acid,concentrated sulfuric acid, concentrated hydrochloric acid,trifluoroacetic acid, phosphoric acid, polyphosphoric acid, phosphorusoxychloride, phosphorus trioxide, phosphorus pentoxide, Lewis acids,aluminum chloride, ferric chloride, zinc chloride, tin chloride,titanium chloride, boron trifluoride, antimony pentachloride andzirconium tetrachloride.
 8. The method of claim 6 wherein the ringclosing reagent is sulfuric acid.
 9. The method of claim 6 furthercomprising the step of heating.
 10. A process for making1-(3-carboxypyridyl-2)-4-methyl-2-phenyl-piperazine by hydrolyzing1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine comprising the step ofreacting 1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine with a basewherein the base is present in a ratio of up to about 12 moles of thebase per one mole of 1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine.11. The process of claim 10 wherein the ratio of the base to1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine is about 12 moles ofbase to about one mole of1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine to about 9 moles ofbase to about one mole of1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine.
 12. The process ofclaim 10 wherein the base is potassium hydroxide or sodium hydroxide 13.The process of claim 12 wherein the mixture of the1-(3-cyanopyridyl-2)-4-methyl-2-phenyl-piperazine and the base is heatedto at least about 130° C.
 14. The process of claim 13 wherein themixture is heated to about 130° C. to about 150° C.
 15. The process ofclaim 12 wherein the hydrolysis is carried out in water and an aproticpolar solvent.
 16. The process of claim 12 wherein the hydrolysis iscarried out in a mixture of water and a solvent selected from the groupconsisting of methanol, ethanol, propanol, isopropanol, butanol,dimethylformamide, dimethylacetamide and dimethylsulfoxide.
 17. Theprocess of claim 12 wherein the hydrolysis is carried out at a pressureof about 3 to about 4 atmospheres pressure.
 18. The process of claim 12wherein the hydrolysis is carried out at almost neat conditions.
 19. Aprocess for recrystallized mirtazapine from crude mirtazapine comprisingthe steps of: (a) heating a mixture of crude mirtazapine and a solvent;(b) cooling the mixture such that purified mirtazapine precipitatis; and(c) isolating the recrystallized mirtazapine.
 20. The process of claim19 wherein the solvent is selected from the group consisting ofmethanol, ethanol, isopropanol, acetone, and mixtures thereof.
 21. Theprocess of claim 20 further comprising the step of adding water to themixture of mirtazapine and solvent to facilitate precipitation ofmirtazapine.
 22. The process of claim 19 where in the solvent isselected from the group consisting of toluene, hexane, and methylenechloride, and mixtures thereof.
 23. The process of claim 20 wherein thesolvent is ethanol.
 24. The process of claim 19 wherein therecrystallized mirtazapine is a mirtazapine water adduct.
 25. Theproduct of the process claim 24 .
 26. Mirtazapine prepared according tothe process of claim 1 .
 27. A pharmaceutical composition comprising atherapeutically effective amount of mirtazapine of claim 26 , and apharmaceutically acceptable carrier.
 28. A method for the treatment ofdepression, comprising the step of administering to a human subject inneed of such treatment the pharmaceutical composition of claim 27 .